Predicted protein targets (top 6)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | STAT3 | P40763 | 1/20 | 0.56 |
| ▸ | STAT1 | P42224 | 1/20 | 0.56 |
| ▸ | TERT | O14746 | 4/20 | 0.34 |
| ▸ | TOP1 | P11387 | 3/20 | 0.32 |
| ▸ | ABCG2 | Q9UNQ0 | 1/20 | 0.31 |
| ▸ | CYCS | P99999 | 1/20 | 0.30 |
Click a target to see other patent compounds predicted against it — the reverse direction, in place.
Similar compounds — the chemically nearest patent molecules
Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| Zinc Ion SCHEMBL30574169 | 0.99 | STAT3 (0.55) | STAT3STAT1TERTTOP1ABCG2 | |
| SCHEMBL31127550 | 0.99 | STAT3 (0.55) | STAT3STAT1TERTTOP1ABCG2 | |
| SCHEMBL6411259 | 0.97 | STAT3 (0.53) | STAT3STAT1TERTTOP1 | |
| SCHEMBL3416778 | 0.96 | STAT3 (0.51) | STAT3STAT1TERTTOP1ABCG2 | |
| SCHEMBL78093 | 0.90 | STAT3 (0.47) | STAT3STAT1TERTTOP1ABCG2 | |
| SCHEMBL93006 | 0.90 | STAT3 (0.47) | STAT3STAT1TERTTOP1ABCG2 | |
| SCHEMBL93007 | 0.90 | STAT3 (0.56) | STAT3STAT1TERTTOP1ABCG2 | |
| SCHEMBL13970977 | 0.89 | STAT3 (0.69) | STAT3STAT1TERTTOP1ABCG2 | |
| SCHEMBL26285585 | 0.89 | STAT3 (0.55) | STAT3STAT1TERTTOP1ABCG2 | |
| SCHEMBL6048211 | 0.89 | STAT3 (0.69) | STAT3STAT1TERTTOP1ABCG2 |
Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.
Patent provenance — the patents this molecule appears in, and who filed them
Claimed or disclosed in 33 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-116715670-A | Metalloporphyrin structure, preparation method thereof and application thereof in preparation of photocatalyst | 江苏大学 | 2023-09-08 | — | — | CN | disclosed |
| CN-113416981-B | Triphenylamine-based cobalt porphyrin catalyst and preparation method and application thereof | 江苏大学 | 2022-06-21 | — | — | CN | disclosed |
| US-20150273457-A1 | HIGHLY ACTIVE MULTIDENTATE CATALYSTS FOR EFFICIENT ALKYNE METATHESIS | NATIONAL SCIENCE FOUNDATION | 2015-10-01 | — | — | US | disclosed |
| US-20150273457-A1 | HIGHLY ACTIVE MULTIDENTATE CATALYSTS FOR EFFICIENT ALKYNE METATHESIS | NATIONAL SCIENCE FOUNDATION | 2015-10-01 | — | — | US | disclosed |
| US-8993804-B2 | Highly active multidentate catalysts for efficient alkyne metathesis | THE REGENTS OF THE UNIVERSITY OF COLORADO, A BODY CORPORATE (US) | 2015-03-31 | — | — | US | disclosed |
| US-8993804-B2 | Highly active multidentate catalysts for efficient alkyne metathesis | THE REGENTS OF THE UNIVERSITY OF COLORADO, A BODY CORPORATE (US) | 2015-03-31 | — | — | US | disclosed |
| US-20130261295-A1 | Highly Active Multidentate Catalysts for Efficient Alkyne Metathesis | THE REGENTS OF THE UNIVERSITY OF COLORADO, A BODY CORPORATE (US) | 2013-10-03 | — | — | US | disclosed |
| US-20130261295-A1 | Highly Active Multidentate Catalysts for Efficient Alkyne Metathesis | THE REGENTS OF THE UNIVERSITY OF COLORADO, A BODY CORPORATE (US) | 2013-10-03 | — | — | US | disclosed |
| US-20120126214-A1 | METHODS AND INTERMEDIATES FOR THE SYNTHESIS OF DIPYRRIN-SUBSTITUTED PORPHYRINIC MACROCYCLES | UNITED STATES DEPARTMENT OF ENERGY | 2012-05-24 | — | — | US | disclosed |
| US-20120126214-A1 | METHODS AND INTERMEDIATES FOR THE SYNTHESIS OF DIPYRRIN-SUBSTITUTED PORPHYRINIC MACROCYCLES | UNITED STATES DEPARTMENT OF ENERGY | 2012-05-24 | — | — | US | disclosed |
| US-7723513-B2 | for production of molecular memory devices, solar cells and light harvesting arrays | NORTH CAROLINA STATE UNIVERSITY (US) | 2010-05-25 | — | — | US | disclosed |
| US-7723513-B2 | for production of molecular memory devices, solar cells and light harvesting arrays | NORTH CAROLINA STATE UNIVERSITY (US) | 2010-05-25 | — | — | US | disclosed |
| US-7723513-B2 | for production of molecular memory devices, solar cells and light harvesting arrays | NORTH CAROLINA STATE UNIVERSITY (US) | 2010-05-25 | — | — | US | disclosed |
| US-7332599-B2 | Reacting a dipyrromethane with an oxidant and a metal salt to produce the bis(dipyrrinato)metal complex; for making molecular memory devices, solar cells and light harvesting arrays | NORTH CAROLINA STATE UNIVERSITY (US) | 2008-02-19 | — | — | US | disclosed |
| US-7332599-B2 | Reacting a dipyrromethane with an oxidant and a metal salt to produce the bis(dipyrrinato)metal complex; for making molecular memory devices, solar cells and light harvesting arrays | NORTH CAROLINA STATE UNIVERSITY (US) | 2008-02-19 | — | — | US | disclosed |
| US-20070191600-A1 | for production of molecular memory devices, solar cells and light harvesting arrays | NORTH CAROLINA STATE UNIVERSITY (US) | 2007-08-16 | — | — | US | disclosed |
| US-20070191600-A1 | for production of molecular memory devices, solar cells and light harvesting arrays | NORTH CAROLINA STATE UNIVERSITY (US) | 2007-08-16 | — | — | US | disclosed |
| US-20070191600-A1 | for production of molecular memory devices, solar cells and light harvesting arrays | NORTH CAROLINA STATE UNIVERSITY (US) | 2007-08-16 | — | — | US | disclosed |
| WO-2004109768-A2 | METHODS AND INTERMEDIATES FOR THE SYNTHESIS OF DIPYRRIN-SUBSTITUTED PORPHYRINIC MACROCYCLES | NORTH CAROLINA STATE UNIVERSITY (US) | 2004-12-16 | — | — | WO | disclosed |
| US-20040254383-A1 | Reacting a dipyrromethane with an oxidant and a metal salt to produce the bis(dipyrrinato)metal complex; for making molecular memory devices, solar cells and light harvesting arrays | UNITED STATE DEPARTMENT OF ENERGY | 2004-12-16 | — | — | US | disclosed |
Patent text — is the patent's own abstract consistent with the prediction?
For each of this compound's patents that has machine-readable text (4 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.
| Patent | Title | Text reads most about | Predicted target · text-rank |
|---|---|---|---|
| US-20150273457-A1 | HIGHLY ACTIVE MULTIDENTATE CATALYSTS FOR EFFICIENT ALKYNE METATHESIS | PCNA, TRIM58, CAD | STAT3 3890/4885STAT1 4442/4885TERT 997/4885 |
| US-20120126214-A1 | METHODS AND INTERMEDIATES FOR THE SYNTHESIS OF DIPYRRIN-SUBSTITUTED PORPHYRINIC MACROCYCLES | HCCS, PPOX, DHPS | STAT3 3766/4885STAT1 4231/4885TERT 739/4885 |
| US-20130261295-A1 | Highly Active Multidentate Catalysts for Efficient Alkyne Metathesis | PCNA, TRIM58, CAD | STAT3 3890/4885STAT1 4442/4885TERT 997/4885 |
| US-20040254383-A1 | Reacting a dipyrromethane with an oxidant and a metal salt to produce the bis(dipyrrinato)metal complex; for making molecular memory devices, solar cells and light harvesting arrays | PPOX, NCS1, CRY1 | STAT3 750/4885STAT1 2028/4885TERT 1167/4885 |
“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.